1) PCR uses double-stranded DNA, DNA polymerase, dNTPs and primers to amplify the DNA large number of DNA copies can be produced via PCR so the answer is c) to make copies of specific regions of DNA.
(the region between the primer binding site are amplified)
2) the DNA is replicated by the Taq polymerase by adding dNTPs complementary to the template strand, to the 3`-OH of the growing nucleic acid, so the answer is b) replication.
3) DNA polymerase can add dNTPs to the 3`-OH of the existing nucleic acid so the replication occurs in the 5 to 3` direction so the answer is c) 3`- hydroxyl of deoxyribose.
4) the DNA is replicated by the Taq polymerase by adding dNTPs complementary to the template strand, to the 3`-OH of the growing nucleic acid, so the answer is b) dNTPs.
5) Mg2+ is a cofactor of the DNA polymerase, DNA polymerase is functional only when it is bound to Mg2+ so the answer is a) act as a cofactor for polymerase.
Carolina Savirana Craz 3/12/20 GECC-Polymerase Chain Reaction 1. What is the purpose of the polymerase chain...
Polymerase Chain Reaction (PCR) uses a special heat-stable DNA polymerase (Taq polymerase) that is slightly less accurate than DNA polymerase (Pol I) purified from E. coli. Taq polymerase will therefore introduce wrong bases into a growing DNA chain more frequently than will Pol I. In which one or more of the following applications of PCR will this type of inaccuracy be a problem? Explain why. Detection of bacterial DNA in infected tissues from patients. Detection of viral RNA in infected...
1) What does PCR stand for and what does it do? a. Polymerase Chain Reaction; PCR deletes DNA b. Polymerase Copying Repeats; PCR amplifies DNA c. Polymerase Copying Releats; PCR deletes DNA d. Polymerase Chain Reaction; PCR amplifies DNA 2) During gel electrophoresis, the DNA fragments are separated by ____ a. charge b. DNA fragments cannot be separated c. color d. size 3) Primers are a. double stranded DNA oligonucleotide (fragment) b. double stranded RNA oligonucleotide (fragment) c. single stranded...
1.The PCR (polymerase chain reaction) protocol that is currently
used in laboratories was facilitated by the discovery of a
bacterium called Thermus aquaticus in a hot spring inside
Yellowstone National Park, in Wyoming. This organism contains a
heat-stable form of DNA polymerase known as Taq
polymerase, which continues to function even after it has been
heated to 95°C.
a.Why would such a heat-stable polymerase be beneficial in
PCR?
b.What would happen if it weren’t
heat stable?
c.How might you choose...
Eliminating which of the following from a PCR reaction would result in no amplification of DNA? a) template DNA b) primers c) Taq Polymerase d) dNTPs e) Eliminating any of these would result in no amplification of DNA
PCR utilizes specific DNA primers and polymerase enzyme to make copies of particular DNA sequence. The primers must attach to separated DNA at the target sequences so that the polymerase can build new DNA strands. What must also be added to the mixture besides primers and polymerase enzyme in order to get amplification and DNA? a. RNA polymerase b. dNTPs c. electron carriers d. DNA repair enzymes
12. To see if your polymerase chain reaction was successful and it amplified the right sequence of interest, you electrophorese the products from the reaction on an agarose gel. After staining the gel you find there are two bands of different sizes. Which one of the following is a possible explanation for these results? (1 point) a. The PCR induced a frame shift mutation into the DNA sequence. b. RNA polymerase copied the DNA into two copies of RNA. c....
Primers are short pieces of DNA that are used in PCR (Polymerase Chain Reaction), the process which is used in molecular labs to make copies of short stretches of a gene or genome. You have designed primes that have a Molecular Weight (MW) of 6000. It arrives as a dry sample in the quantity of 300 µg. How much water do you need to add to make a primer stock solution of 100 mM primers? HINTS: Remember that mM is...
Which of the following statements about Polymerase Chain Reactions is wrong? a. DNA is briefly heated to break the hydrogen bonds holding two strands together. b. Primers hybridize to sequences at opposite ends of the target sequence on the same strand. c. DNA is cooled to allow primers to form hydrogen bonds with the ends of the target sequence. d. The three steps of PCR are denaturation, annealing, and extension. e. PCR produces specific DNA fragments for cloning. f. Taq...
Now. you should be able to answer the following questions: • How the amplification will be done? - How you will determine your target sequence? How the amplification will be specific for certain segment? What are the requirements to carry PCR? • Suppose you perform a PCR that begins with one double-strand of the following DNA template: +5'-CTACCTGCGGGTTGACTGCTACCTTCCCGGGATGCCCAAAATTCTCGAG-3+ +3'-GATGGACGCCCAACTGACGATGGAAGGGCCCTACGGGTTTTAAGAGCTC-5'+ A. Draw one cycle of PCR reaction below the following diagram. B. Label the template DNA, the primers, and what is...
20- In cheek DNA extraction procedure, what is the purpose of heating a. To speed up the DNA precipitation b. To hydrolyze protein content c. To lysis cell d. To separate DNA fragments 21- What is the reason of using Taq DNA Polymerase in most of the PCR reactions. a. Taq polymerase is sensitive to high temperature b. Taq is very cheep to produce c. Taq can tolerate DNA denaturation temperature d. a, and b Assay questions 5 points each...